Medigroup, Inc.

Medigroup, Inc. — FDA 510(k) Submissions

Medigroup, Inc. has submitted 6 FDA 510(k) premarket notifications since 1998, of which 4 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Catheter, Peritoneal, Long-term Indwelling, Catheter, Peritoneal Dialysis, Single Use . Use the specialty filter in the sidebar to narrow results.